3mhz

1.7A structure of 2-fluorohistidine labeled Protective Antigen

Method: X-RAY DIFFRACTION Dmax: 113.4 Å Quality: REASONABLE

1. Protein Identity and Related Structures Protein Identity & Related Structures

Protective antigen

Bacillus anthracis

UniProt P13423

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 30–764 Non-standard monomer:Yes (specific site not provided by mmCIF) CA CALCIUM ION × 2 PG4 TETRAETHYLENE GLYCOL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION;pH 8.2;293 K;30% PEG 400, 0.1M Tris, pH 8.2, vapor diffusion, temperature 293K Resolution 1.70 Å R-free 0.222

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

28 other PDB entries and 42 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PAG_BACAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–735; UniProt 30–764

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 3mhz

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3mhz
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3mhz
Deposition date deposition_date2010-04-09
Structure title title1.7A structure of 2-fluorohistidine labeled Protective Antigen
Keywords keywordsanthrax, toxin, 2-fluorohistidine, pore, histidine, receptor, hydrogen bonding; TOXIN
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier32.90
Radius of gyration Rg (electron density) rg_electron32.64
Forward intensity I(0) i090551700.00
Molecular weight molecular_weight75142.0 kDa
Excluded volume excluded_volume93792 ų
Envelope volume envelope_volume122090 ų
Hydration-shell volume shell_volume33118 ų
Envelope diameter envelope_diameter118.3
Shell Rg shell_rg37.08
Envelope Rg envelope_rg32.89
Shape Rg shape_rg32.66
Total Rg total_rg32.95
Total atoms total_atoms5296
Residues n_residues666
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax113.4
Rg (real space) rg_real33.21
Rg uncertainty (real space) rg_real_error1.50
I(0) (real space) i0_real9.0550e+07
I(0) uncertainty (real space) i0_real_error1.6770e+06
Rg (reciprocal space) rg_reciprocal33.08
I(0) (reciprocal space) i0_reciprocal90540000.0000
Solution quality estimate total_estimate0.6232
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.7
Skewness Skewness skewness0.508
Kurtosis Kurtosis kurtosis-0.326
Angular range angular_range— – 0.2400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha27470000.0000
Real-space data points n_real_points49
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.783; Stabil: 0.999; Sysdev: 0.049; Positv: 1.000; Valcen: 0.761; Smooth: 0.841

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3mhza1
Class classf — Membrane and cell surface proteins and peptides
Fold Fold foldf.60 — Anthrax protective antigen C-terminal-like
Superfamily Superfamily superfamilyf.60.1 — Anthrax protective antigen C-terminal-like
Family Family familyf.60.1.1 — Anthrax protective antigen C-terminal-like
Domain ID domain_idd3mhza2
Class classb — All beta proteins
Fold Fold foldb.179 — Anthrax protective antigen N-terminal-like
Superfamily Superfamily superfamilyb.179.1 — PA14-like
Family Family familyb.179.1.1 — PA14

CATH v4.4 (4 domains)

Domain ID domain_id3mhzA01
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology182 — Toxin - Anthrax Protective Antigen; domain 1
Homologous superfamily homologous superfamily10 — Toxin - Anthrax Protective Antigen;domain 1
Domain ID domain_id3mhzA02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily240 — Protective antigen, heptamerisation domain
Domain ID domain_id3mhzA03
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily110
Domain ID domain_id3mhzA04
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily810

8. Citations (1)

9. Files and Curves (10)